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Items: 10

1.

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations.

Shimazaki H, Takiyama Y, Sakoe K, Ikeguchi K, Niijima K, Kaneko J, Namekawa M, Ogawa T, Date H, Tsuji S, Nakano I, Nishizawa M.

Neurology. 2002 Aug 27;59(4):590-5.

PMID:
12196655
2.

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1.

Tada M, Yokoseki A, Sato T, Makifuchi T, Onodera O.

Adv Exp Med Biol. 2010;685:21-33. Review.

PMID:
20687492
3.

[Clinical features and molecular genetics of autosomal recessive spinocerebellar degenerations].

Tsuji S.

Rinsho Shinkeigaku. 2004 Nov;44(11):785-7. Review. Japanese.

PMID:
15651291
4.

Spinocerebellar ataxia with ocular motor apraxia and DNA repair.

Onodera O.

Neuropathology. 2006 Aug;26(4):361-7. Review.

PMID:
16961074
5.

Autosomal recessive cerebellar ataxias.

Palau F, Espinós C.

Orphanet J Rare Dis. 2006 Nov 17;1:47. Review.

6.

Short-patch single-strand break repair in ataxia oculomotor apraxia-1.

Reynolds JJ, El-Khamisy SF, Caldecott KW.

Biochem Soc Trans. 2009 Jun;37(Pt 3):577-81. doi: 10.1042/BST0370577. Review.

PMID:
19442253
7.

Spinocerebellar ataxia 13 and 25.

Stevanin G, Dürr A.

Handb Clin Neurol. 2012;103:549-53. doi: 10.1016/B978-0-444-51892-7.00035-8. Review.

PMID:
21827913
8.

Primary degeneration of the granular layer of the cerebellum. A study of 14 patients and review of the literature.

Pascual-Castroviejo I, Gutierrez M, Morales C, Gonzalez-Mediero I, Martínez-Bermejo A, Pascual-Pascual SI.

Neuropediatrics. 1994 Aug;25(4):183-90. Review.

PMID:
7824090
9.

Late-onset pure cerebellar ataxia: differentiating those with and without identifiable mutations.

Kerber KA, Jen JC, Perlman S, Baloh RW.

J Neurol Sci. 2005 Nov 15;238(1-2):41-5. Epub 2005 Aug 16. Review.

PMID:
16109427
10.

Congenital ocular motor apraxia. Case reports and literature review.

PeBenito R, Cracco JB.

Clin Pediatr (Phila). 1988 Jan;27(1):27-31. Review.

PMID:
3275520

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